Casa Marzam SA de CV
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
Дистрибьютор комплексных медицинских товаров и лекарств, обслуживающий клиентов розничных аптек.
Casa Marzam S.A. de C.V. занимается поставками товаров медицинского назначения, отслеживает распространение фармацевтических препаратов и потребительских товаров для здоровья. Компания предоставляет оптимизированные решения по поставкам для частных медицинских учреждений и супермаркетов. Их архитектура распределения обеспечивает точный контроль температуры во время транспортных циклов.
- Type
- Not established by any record (our catalog import lists it as distributor; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Mexico City, Mexico
- Founded
- 1934 (from our catalogue record; not confirmed by the company or by a state register)
- Website
- marzam.com.mx
- Categories
- Медицинские товары и расходники, Средства личной гигиены
- Markets
- Мексика
What is established and what is not
No researcher review has been written for this company yet. 2 official records from 2 official sources are on file. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. Nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Legal entity ID lapsed (record type: lei-lapsed) [official record; status amber] The global finance identifier was not renewed. checked 2026-09-07. GLEIF global LEI register (golden copy)
- Registry ID checks out with the state register (record type: registry-id-verified) [official record; status green] Helps confirm the company on this page is the same legal entity as in the register. checked 2026-09-10. GLEIF Global LEI record
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
Goods family established: Медицинские товары и расходники (the company's own text). The exact product, operation and trade route needed to determine a product-specific requirement are not established here. Product-specific import rules not established for the catalog category Средства личной гигиены: no record or company text names goods of this kind. A catalog category alone is our classification, not proof of what the company makes or sells.
Check independently
Before a first order, ask whose products they sell and on what basis: a distribution agreement or the manufacturer's authorisation.